Un estudio para evaluar los eventos adversos y el cambio en la actividad de la enfermedad de ABBV-324 infundido por vía intravenosa (IV) en participantes adultos con cáncer hepatocelular (CHC) o cáncer de pulmón de células no pequeñas de células escamosas (LUSC)
Un primer estudio de fase 1 en humano que evalúa la seguridad, la farmacocinética y la eficacia de ABBV 324 en adultos con cáncer hepatocelular o cáncer de pulmón de células escamosas de células escamosas
HCC is a common cancer worldwide and a leading cause of cancer-related death. Lung cancer is the most frequently diagnosed cancer in the world, and the leading cause of cancer deaths. The purpose of this study is to assess adverse events and change in disease activity when ABBV-324 is given to adult participants to treat hepatocellular cancer (HCC) or squamous-cell non-small cell lung cancer (LUSC).
ABBV-324 is an investigational drug being developed for the treatment of HCC and LUSC. Study doctors put the participants in groups called arms. Each arm receives ABBV-324 alone (monotherapy) or a comparator drug, lenvatinib followed by a safety follow-up period. Approximately 232 HCC or LUSC will be enrolled in the study in approximately 45 sites worldwide.
In the dose escalation stage participants will be treated with increasing intravenous (IV) doses of ABBV-324 until the dose reached is tolerable and expected to be efficacious. In the dose optimization stage participants will receive ABBV-324, or a comparator of oral lenvatinib. The study will run for a duration of approximately 6.5 years.
There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at an approved institution (hospital or clinic). The effect of the treatment will be frequently checked by medical assessments, blood tests, questionnaires and side effects.
Descripción general del estudio
Estado
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: ABBVIE CALL CENTER
- Número de teléfono: 844-663-3742
- Correo electrónico: abbvieclinicaltrials@abbvie.com
Ubicaciones de estudio
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Madrid, España, 28040
- Reclutamiento
- Hospital Universitario Fundacion Jimenez Diaz /ID# 272718
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Madrid, España, 28050
- Reclutamiento
- Hospital Universitario HM Sanchinarro /ID# 272719
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California
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Duarte, California, Estados Unidos, 91010
- Reclutamiento
- City of Hope National Medical Center /ID# 270526
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Irvine, California, Estados Unidos, 92618
- Reclutamiento
- City of Hope - Orange County Lennar Foundation Cancer Center /ID# 276120
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Los Angeles, California, Estados Unidos, 90033
- Reclutamiento
- USC Norris Comprehensive Cancer Center /ID# 271573
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Orange, California, Estados Unidos, 92868
- Reclutamiento
- University Of California Irvine Medical Center /ID# 270507
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Santa Monica, California, Estados Unidos, 90404
- Reclutamiento
- UCLA - Santa Monica /ID# 275995
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Illinois
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Chicago, Illinois, Estados Unidos, 60637
- Reclutamiento
- University of Chicago Medical Center /ID# 270517
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Missouri
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St Louis, Missouri, Estados Unidos, 63110
- Reclutamiento
- Washington University /ID# 275757
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New York
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New York, New York, Estados Unidos, 10021-3459
- Reclutamiento
- Memorial Sloan Kettering Cancer Center /ID# 271228
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Pennsylvania
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Philadelphia, Pennsylvania, Estados Unidos, 19107
- Reclutamiento
- Thomas Jefferson University Sidney Kimmel Cancer Center /ID# 276269
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Tennessee
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Nashville, Tennessee, Estados Unidos, 37203
- Reclutamiento
- SCRI Oncology Partners /ID# 272750
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Haifa, Israel, 3109601
- Reclutamiento
- Rambam Health Care Campus /ID# 270604
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Jerusalem, Israel, 91120
- Reclutamiento
- Hadassah Medical Center-Hebrew University /ID# 271235
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Central District
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Petah Tikva, Central District, Israel, 4941492
- Reclutamiento
- Rabin Medical Center. /ID# 271236
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Chiba
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Kashiwa-shi, Chiba, Japón, 277-8577
- Reclutamiento
- National Cancer Center Hospital East /ID# 270585
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Osaka
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Hirakata-shi, Osaka, Japón, 573-1191
- Reclutamiento
- Kansai Medical University Hospital /ID# 272884
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Tokyo
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Chuo-Ku, Tokyo, Japón, 104-0045
- Reclutamiento
- National Cancer Center Hospital /ID# 270583
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Guangdong
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Guangzhou, Guangdong, Porcelana, 510000
- Reclutamiento
- Nanfang Hospital - Southern Medical University /ID# 276916
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Porcelana, 200032
- Reclutamiento
- Zhongshan Hospital Fudan University /ID# 276917
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San Juan, Puerto Rico, 00927
- Terminado
- Fdi Clinical Research /ID# 272960
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Taipei, Taiwán, 100
- Reclutamiento
- National Taiwan University Hospital /ID# 270593
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
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Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
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Hepatocellular cancer (HCC) only: Child-Pugh A classification within 7 days before Cycle 1, Day 1 dosing.
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Laboratory values meeting the criteria outlined in the protocol.
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QT interval corrected for heart rate (QTc) < 470 msec (using Fridericia's correction), no Grade 3 arrythmia, and no other clinically significant cardiac abnormalities.
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Measurable disease per RECIST version 1.1.
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Part 1 and Part 2 - participants with HCC meeting the following disease activity criteria:
- Locally advanced or metastatic and/or unresectable HCC with diagnosis confirmed by histology or cytology. Participants with fibrolamellar HCC, sarcomatoid HCC, or mixed cholangiocarcinoma/HCC are not eligible to enroll.
- Disease that is not amenable to surgical and/or locoregional therapies, or progressive disease after surgical and/or locoregional therapies. For participants who progressed after locoregional therapy for HCC, locoregional therapy must have been completed >= 28 days prior to baseline scan for the current study.
- Part 1: Failure of at least 1 prior systemic treatment for HCC.
- Part 2: Failure of at least 1 prior systemic treatment consisting of an immune checkpoint inhibitor (CPI) containing regimen for HCC, including but not limited to, atezolizumab in combination with bevacizumab or tremelimumab in combination with durvalumab. Note: Participants who have received prior lenvatinib will not be eligible for Part 2.
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Part 1 only - participants with squamous-cell non-small cell lung cancer (LUSC) meeting the following disease activity criteria:
- Advanced or metastatic LUSC that is not amenable to surgical resection.
- Must have failed at least 1 prior line of therapy that included at least platinum-based chemotherapy and an immune CPI, and/or an appropriate targeted therapy (if applicable), or is not suitable for other approved therapeutic options that have demonstrated clinical benefit at the judgment of the investigator. Participants should have no more than 2 lines of prior cytotoxic chemotherapy excluding neoadjuvant and/or adjuvant. Participants who are intolerant of standard therapy are eligible.
Exclusion Criteria:
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Unresolved clinically significant adverse events (AEs) > Grade 1 from prior anticancer therapy except for alopecia.
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Untreated brain or meningeal metastases (i.e., participants with history of metastases are eligible provided they do not require ongoing steroid treatment for cerebral edema and have shown clinical and radiographic stability for at least 14 days after definitive therapy). Participants may continue with antiepileptic therapy if required.
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History of interstitial lung disease (ILD) or pneumonitis that required treatment with systemic steroids, or any evidence of active ILD or pneumonitis on screening chest computed tomography (CT) scan.
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History of idiopathic pulmonary fibrosis, organizing pneumonia (e.g., bronchiolitis obliterans), drug-induced pneumonitis, or idiopathic pneumonitis.
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History of clinically significant, intercurrent lung-specific illnesses including, but not limited to:
- Underlying pulmonary disorder (i.e., pulmonary emboli within 3 months of the study enrollment, severe asthma, severe COPD, restrictive lung disease, pleural effusion, dependence on supplemental oxygen, etc.).
- Any autoimmune, connective tissue or inflammatory disorders with documented or suspicious pulmonary involvement at Screening.
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Must have discontinued anticancer therapy with antineoplastic intent including chemotherapy, radiation therapy, immunotherapy, biologic, or any investigational therapy within 14 days or 5 half lives of the drug (whichever is shorter) prior to the first dose of ABBV-324. Palliative radiation therapy for bone, skin or subcutaneous metastases with 10 fractions or less is permitted and not participant to a washout period.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación Secuencial
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Part 1 Dose Escalation: ABBV-324
Participants will receive escalating doses of ABBV-324 as part of the approximately 6.5 year study duration. |
Intravenous (IV) Infusion |
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Experimental: Part 2 Dose Optimization Arm 1: ABBV-324 Dose 1
Participants will receive ABBV-324 dose 1 as part of the approximately 6.5 year study duration. |
Intravenous (IV) Infusion |
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Experimental: Part 2 Dose Optimization Arm 1: ABBV-324 Dose 2
Participants will receive ABBV-324 dose 2 as part of the approximately 6.5 year study duration. |
Intravenous (IV) Infusion |
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Experimental: Part 2 Dose Optimization Arm 1: ABBV-324 Dose 3
Participants will receive ABBV-324 dose 3 as part of the approximately 6.5 year study duration. |
Intravenous (IV) Infusion |
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Comparador activo: Part 2 Comparator Arm 4: Lenvatinib
Participants will receive lenvatinib as part of the approximately 6.5 year study duration. |
Oral Capsule |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Number of Participants with Adverse Events (AE)s
Periodo de tiempo: Up to Approximately 4 Years
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An adverse event is defined as any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and which does not necessarily have a causal relationship with this treatment. |
Up to Approximately 4 Years
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Number of Participants with Change in Vital Signs
Periodo de tiempo: Up to Approximately 4 Years
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Number of Participants with Change in Vital Signs will be assessed. |
Up to Approximately 4 Years
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Number of Participants with Change in Electrocardiogram (ECG)
Periodo de tiempo: Up to Approximately 4 Years
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Number of Participants with Change in ECG will be assessed. |
Up to Approximately 4 Years
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Number of Participants with Change in Clinical Laboratory Tests
Periodo de tiempo: Up to Approximately 4 Years
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Number of participants with change in clinical laboratory tests will be assessed. |
Up to Approximately 4 Years
|
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Objective Response Rate (ORR)
Periodo de tiempo: Up to Approximately 4 Years
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ORR is defined as the percentage of participants with a confirmed Complete Response or partial response(PR) per investigator review according to response evaluation criteria in solid tumors (RECIST) version 1.1. |
Up to Approximately 4 Years
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Area Under the Serum Concentration Versus Time Curve (AUC) of ABBV-324
Periodo de tiempo: Up to Approximately 4 Years
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AUC of ABBV-324. |
Up to Approximately 4 Years
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Maximum Observed Serum Concentration (Cmax) of ABBV-324
Periodo de tiempo: Up to Approximately 4 Years
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Cmax of ABBV-324. |
Up to Approximately 4 Years
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Time to Maximum Observed Serum Concentration (Tmax) of ABBV-324
Periodo de tiempo: Up to Approximately 4 Years
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Tmax of ABBV-324. |
Up to Approximately 4 Years
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Terminal Elimination Half-Life (t1/2) of ABBV-324
Periodo de tiempo: Up to Approximately 4 Years
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t1/2 of ABBV-324. |
Up to Approximately 4 Years
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Antidrug Antibody (ADA)
Periodo de tiempo: Up to Approximately 4 Years
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Incidence and concentration of anti-drug antibodies. |
Up to Approximately 4 Years
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Neutralizing Antidrug Antibody (nADA)
Periodo de tiempo: Up to Approximately 4 Years
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Incidence and concentration of neutralizing anti-drug antibodies. |
Up to Approximately 4 Years
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Director de estudio: ABBVIE INC., AbbVie
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- M25-292
- 2024-518012-39 (Otro identificador: EU CT)
- 2024-518012-39-00 (Ctis)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
producto fabricado y exportado desde los EE. UU.
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